Biomet SpinalPak Non-invasive Spine Fusion Stimulator System
- Highest overall success rate in lumbar fusions - 84.7% (inclusive of ALIF, PLIF, posterolateral and combo)
- 270,000 patients treated to date
- 75% of Biomet customers are repeat prescribers
Pre-clinical studies have shown that Capacitive Coupling causes significantly higher levels of cellular proliferation than other electrical stimulation technologies
In vitro pre-clinical studies upregulation of multiple BMPs in as little as 30 minutes of exposure with optimal upregulation at 24 hours of exposure4
In a double-blind study, patients experienced a 20% improvement over placebo; use of the device may reduce the need for revision surgery
Smallest and lightest bone growth stimulation device on the market, designed with active patients in mind
Compliance monitoring, educational resources and Biomet Alerts program
The Biomet SpinalPak Non-invasive Spine Fusion Stimulator System is a noninvasive bone growth stimulator indicated as an adjunct electrical treatment to primary lumbar spinal fusion surgery for one or two levels. - P850022/S017.
Federal Law (U.S.A.) restricts this device to sale by or on the order of a physician. Rx Only - Prescription Only - Single Patient Use Only - Do Not Reuse.